传统PCI
蛋白质C
表位
单克隆抗体
分子生物学
化学
凝结
抗体
生物化学
医学
生物
免疫学
内科学
心肌梗塞
作者
Karin Strandberg,Margareta Kjellberg,Richard Knebel,Hans Lilja,Johan Stenflo
出处
期刊:Thrombosis and Haemostasis
[Georg Thieme Verlag KG]
日期:2001-01-01
卷期号:86 (08): 604-610
被引量:40
标识
DOI:10.1055/s-0037-1616093
摘要
Summary Activated protein C (APC) is a serine proteinase that regulates blood coagulation. In plasma it is inhibited mainly by the protein C inhibitor (PCI). The plasma concentrations of APC-PCI complex is increased in hypercoagulative states such as deep venous thrombosis. Formation of the APC-PCI complex induces a drastic conformational change in PCI that exposes new epitopes (neoepitopes) on the molecule. We have devised a simple immunofluorometric sandwich assay for measurements of the concentrations of APC-PCI complex, employing as the catcher, a monoclonal antibody that has a high affinity (KD ≈ 4 × 10-11M) for a complexation-specific neoepitope that is expressed on PCI. A monoclonal antibody against protein C is employed as the tracer. The method gives a linear dose-response curve (0.06-50 πg/l), has a low detection limit (0.06 πg/l) and no crossreactivity with native PCI at physiologic plasma concentrations. We have now determined the concentration of the APC-PCI complex in healthy individuals.
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